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Muscular Dystrophy, Duchenne

Known as: Cardiomyopathy, Dilated, X-Linked, x-linked muscular dystrophy, Pseudohypertrophic Childhood Muscular Dystrophy 
An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
BackgroundNo previous systematic review has quantitatively examined the association between muscular fitness during childhood and… Expand
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Highly Cited
2016
Highly Cited
2016
Editing can help build stronger muscles Much of the controversy surrounding the gene-editing technology called CRISPR/Cas9… Expand
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Highly Cited
2011
Highly Cited
2011
The purpose of this Position Stand is to provide guidance to professionals who counsel and prescribe individualized exercise to… Expand
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Highly Cited
2011
Highly Cited
2011
Summary Background We report clinical safety and biochemical efficacy from a dose-ranging study of intravenously administered AVI… Expand
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Highly Cited
1999
Highly Cited
1999
Emery-Dreifuss muscular dystrophy (EDMD) is characterized by early contractures of elbows and Achilles tendons, slowly… Expand
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Highly Cited
1991
Highly Cited
1991
ALTHOUGH murine X-linked muscular dystrophy (mdx) and Duchenne muscular dystrophy (DMD) are genetically homologous and both… Expand
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Highly Cited
1989
Highly Cited
1989
The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy. In both mouse and man the… Expand
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Highly Cited
1988
Highly Cited
1988
The application of recombinant DNA technology to prenatal diagnosis of many recessively inherited X-linked diseases is… Expand
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Highly Cited
1987
Highly Cited
1987
The protein product of the human Duchenne muscular dystrophy locus (DMD) and its mouse homolog (mDMD) have been identified by… Expand
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Highly Cited
1987
Highly Cited
1987
The 14 kb human Duchenne muscular dystrophy (DMD) cDNA corresponding to a complete representation of the fetal skeletal muscle… Expand
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